A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601903



Internal ID16042626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31489801hg38UCSC Ensembl
Innerchr6:31360389..31457578hg19UCSC Ensembl
Innerchr6:31468368..31565557hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3897190
hg1997190
hg1897190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10454n54
Supporting Variantsnssv1154281, nssv1053473, nssv1053474, nssv1053475
SamplesNINDS_192
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601903
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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